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首页> 外文期刊>Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer >A randomized phase II trial of pemetrexed/gemcitabine/bevacizumab or pemetrexed/carboplatin/bevacizumab in the first-line treatment of elderly patients with advanced non-small cell lung cancer.
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A randomized phase II trial of pemetrexed/gemcitabine/bevacizumab or pemetrexed/carboplatin/bevacizumab in the first-line treatment of elderly patients with advanced non-small cell lung cancer.

机译:在一系列晚期非小细胞肺癌的老年患者的一线治疗中,培养基/吉西他滨/贝伐单抗或磷酸盐/卡铂/贝伐单抗的随机期II试验。

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PURPOSE: To assess time to progression (TTP) in elderly patients with previously untreated nonsquamous non-small cell lung cancer treated with pemetrexed/gemcitabine/bevacizumab or pemetrexed/carboplatin/bevacizumab. METHODS: Eligible patients were aged 70 years or older with newly diagnosed stage IIIB/IV nonsquamous non-small cell lung cancer; Eastern Cooperative Oncology Group performance status 0 to 1; adequate organ function; and no active central nervous system metastasis. Patients were randomized 1:1 to cohort A (pemetrexed 500 mg/m2 IV, gemcitabine 1500 mg/m2 IV, and bevacizumab 10 mg/kg IV; days 1 and 15 of 28-day cycles) or cohort B (pemetrexed 500 mg/m2 IV, carboplatin area under the concentration-time curve =5 IV, and bevacizumab 15 mg/kg IV; day 1 of 21-day cycles). After six cycles, stable/responding patients continued bevacizumab until disease progression. RESULTS: Between March 2007 and December 2009, 110 patients (median age, 76 years; 88% stage IV) were treated for medians of 2.5 cycles (cohort A) and 6 cycles (cohort B). Overall response rate was 35% in both cohorts, with stable disease rates of 33% (A) and 45% (B). TTP by cohort was 4.7 and 10.2 months with median OS 7.5 and 14.8 months, respectively. Severe toxicities included the following: neutropenia (A, 51% and B, 45%), fatigue (A, 36% and B, 18%), anemia (A, 22% and B, 7%), infection (A, 25% and B, 7%), thrombocytopenia (A, 11% and B, 31%), and thromboembolism (A, 7% and B, 7%). Three potential treatment-related deaths occurred in cohort A (sepsis, thrombocytopenia, and myocardial infarction) and two in B (sepsis and pulmonary hemorrhage). CONCLUSIONS: Treatment with pemetrexed/carboplatin/bevacizumab was associated with improved TTP and OS in this elderly population and should be further evaluated. Treatment-related toxicities were expected and usually manageable, although deaths occurred with both regimens.
机译:目的:为了评估时间老年患者​​进展时间(TTP)与培美曲塞/吉西他滨/贝伐单抗或培美曲塞/卡铂/贝伐单抗治疗先前未治疗的非鳞状非小细胞肺癌。方法:符合条件的患者年龄70岁以上的初诊IIIB / IV期非鳞状非小细胞肺癌;东部肿瘤协作组性能状态0到1;充足的器官功能;和无活性的中枢神经系统转移。患者被随机分为1:1至队列A(培美曲塞500毫克/平方米IV,吉西他滨1500毫克/平方米IV,和贝伐单抗10mg / kg的IV; 1天和第28天的周期15)或队列B(培美曲塞500毫克/平方米IV,在浓度 - 时间曲线= 5 IV下卡铂区域,和贝伐单抗15mg / kg的IV;天的21天周期1)。六个周期后,稳定/应答患者继续贝伐单抗直至疾病进展。结果:2007年3月和2009年12月,110周之间的患者(中位年龄76岁; 88%阶段IV)共治疗的2.5个周期(队列A)和6个周期(队列B)中位数。总体反应率在两个队列35%,33%(A)和45%(B)稳定的疾病率。 TTP通过队列为4.7和10.2个月,中位OS​​ 7.5和14.8个月。严重毒性包括以下内容:中性粒细胞减少(A,51%和B,45%),疲劳(A,36%和B,18%),贫血(A,22%和B,7%),感染(A,25 %和B,7%),血小板减少(A,11%和B,31%),和血栓栓塞(A,7%和B,7%)。三个潜在的治疗相关的死亡发生在队列A(败血症,血小板减少和心肌梗死)和两个B(败血症和肺出血)。结论:治疗培美曲塞/卡铂/贝伐单抗与改进TTP和操作系统在这个老年人口相关联,并应进一步评估。治疗相关毒性预期,通常管理的,虽然死亡与两种方案的发生。

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